Clinical trial
Breathing & Blood Pressure
Recruiting now · Not applicable · 1 countries · Registry ID NCT05632406
Recruiting nowNot applicableObservational
What this study is about
The purpose of this study is to determine the effect of obesity on cardiovascular responses during various breathing maneuvers.
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age18 Years to 45 Years
SexAll
Healthy volunteersAccepted
ConditionHealthy, Overweight and Obesity
Full registry criteria
Inclusion Criteria: • Body mass index values of ≤40 kg/m\^2 Exclusion Criteria: * Not weight stable (\<5% change in body mass over the past six months) * Overt cardiovascular, neurological, renal, liver, and/or metabolic illness (e.g., diabetes mellitus) * Current, or history of uncontrolled, Stage 2 hypertension (blood pressure \>140 / 90 mmHg; anti-hypertensive medications are permitted) * Diagnosed obstructive sleep apnea * Previous bariatric surgery * Diagnosis or signs (e.g., values below the lower limit of normal) of overt airway disease(s) * Current or recent (regular use within the past 6 months) use of tobacco or nicotine products (e.g., cigarettes, vaping) * Per the POWERbreathe® company: * Patients who have undergone recent abdominal surgery and those with abdominal hernia. * Asthma patients who have a very low symptom perception and suffer from frequent, severe exacerbations or with an abnormally low perception of dyspnoea. * If a patient is suffering from a ruptured eardrum or any other condition of the ear. * Patients with marked elevated left ventricular end-diastolic volume and pressure. * Patients with worsening heart failure signs and symptoms after a respiratory/inspiratory muscle training (IMT) session * If you are suffering from a cold, sinusitis, or respiratory tract infection, we advise that you do not use your POWERbreathe IMT device. * Individuals who are not yet adults (infants, children, teenagers) * Pregnant (self-reported and urine pregnancy test conducted), lactating (self-reported), or post-menopausal (self-reported) females * Prisoners
Treatments and study arms
The registry does not list a named intervention.
Primary outcomes
Blood pressure during exerciseUp to one week
Systolic and diastolic blood pressure measured in the laboratory at rest and during an incremental aerobic exercise test
Study locations
1 locations were listed when this page was built. The first 40 are shown.
Florida State University🇺🇸 Tallahassee, Florida, United States
Joseph Watso, PhDContact